Process for a preparation of the modified porcine plasma fibronectin for enhance wound healing

ABSTRACT

This invention reveals the potential applications of modified porcine plasma fibronectin that could be applied as a safe material for clinical wound healing and tissue repair. In order to seek safe sources of plasma fibronectin for practical consideration in wound dressing, this invention isolated and modified fibronectin from porcine plasma and demonstrated that modified porcine plasma fibronectin has similar ability as homo plasma fibronectin being as a suitable substrate for stimulation of cell adhesion and directed cell migration. The present invention also reveals a material and a pharmaceutical composition enhance wound healing.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional Application of co-pending application Ser. No. 15/713,113, filed on Sep. 22, 2017; and this application claims priority of U.S. Provisional Patent Application No. 62/399,688, entitled “Fibronectin in cell adhesion and migration via N-glycosylation,” filed Sep. 26, 2016, which is incorporated herein by reference for all purposes.

FIELD OF THE INVENTION

The present invention relates to a preparation of modified porcine plasma fibronectin that could be applied as a safe material for clinical wound healing and tissue repair. The present invention also reveals a material and a pharmaceutical composition enhance wound healing.

BACKGROUND OF THE INVENTION

Wound healing is a dynamic process, which consists of hemostasis, inflammation, proliferation and remodeling. Fibronectin, an extracellular matrix (ECM) glycoprotein, plays important roles in different stages of wound healing, with the main function being cellular adhesion and mediation of cell migration. Fibronectin interacts and activates cell surface integrin receptors, which in turn recruits a series of cellular proteins to connect with the actin cytoskeleton inside the cell, initiating the formation of integrin based adhesive organelles, focal adhesions (FAs). The coupling of actin cytoskeleton and ECM fibronectin via FAs dynamically drives directed cell migration in wound healing. At the beginning, cell protrusions characterized by actin polymerization into dense actin network are extended in the direction of migration followed by attachment of the protrusions to ECM fibronectin that forms nascent adhesions (new-born FAs). Subsequently, nascent adhesions become matured and growing in size via myosin II-mediated contractile forces transduced along the bundled actin filaments. Mature FAs transduce contractile forces from the actin cytoskeleton to the ECM fibronectin, thereby pulling the cell body forward. Finally, FA disassembly accompanied with myosin II-driven contractile forces retracts the trailing edge of the cell from the ECM fibronectin. The ECM fibronectin outside the cell links to the actin cytoskeleton inside the cell via FAs in association with the dynamic control of cell adhesion and directed cell migration in wound healing.

There are two forms of fibronectin: plasma fibronectin and cellular fibronectin. Plasma fibronectin is synthesized by hepatocytes into the blood plasma, while cellular fibronectin is produced by many cell types such as fibroblasts, endothelial cells, myocytes and chondrocytes. In wound healing, it has been reported that plasma fibronectin accumulates remarkably in the wound after wounding in vivo, which is crucial for various functions of platelets, fibroblasts and endothelial cells such as adhesion, migration and aggregation, revealing that plasma fibronectin is likely to serve as a suitable substrate to accelerate wound repair in vivo. Indeed, in animal model, provisional matrix containing plasma fibronectin significantly supports epidermal cell adhesion and migration in the re-epithelialization process, showing the clinical potential of plasma fibronectin in human wound healing and tissue repair.

However, the application of plasma fibronectin to human wound healing has not been validated due to the unreliable and expensive sources of human plasma. The fibronectin from human is not suitable for use in medical products because the fibronectin in a cancer patient has a specific abnormal glycosylation modification, which has the effect of promoting cancer metastasis. Therefore, it will lead to medical risks that use the high purity fibronectin from the blood of unknown health donors to other people.

In previous publications, the method includes the recombinant of fibronectin proteins by gene recombination and the purification of fibronectin from human blood is flawed. The inventor has demonstrated that the glycans on fibronectin plays an important role in promoting the progress of wound healing, whereas fibronectin, which is expressed by gene recombination, does not contain glycosylation modification, so its effect is a gap.

SUMMARY OF THE INVENTION

Given the importance of plasma fibronectin to wound healing and its potentials in medical application, the inventor set to isolate and modify fibronectin from porcine (porcine plasma fibronectin). The inventor has confirmed that porcine plasma fibronectin can be substitute for human plasma fibronectin to wound healing with better safety and quantity.

As mentioned earlier, the purified fibronectin from human blood has safety concerns, and in our study also found that human fibronectin and porcine fibronectin with similar N-glycan structures on different N-glycosylation sites, and the function are similar.

With further improvement, the development of porcine fibronectin in medical applications can be substitute for human fibronectin with better function and solve the problem from human fibronectin. The inventor has characterized the N-glycosylation sites and N-glycan structures on homo and porcine plasma fibronectin. The inventor found that N-glycans on plasma fibronectin have a role in positive regulation of cell adhesion and directed cell migration by synergistically promoting integrin-mediated adhesive signals. Therefore, to maintain the glycans on plasma fibronectin during the purification procedure is important. However, in previous published method of the fibronectin purification is too rough and without description of glycans preservation either. So, the invention of process for a preparation of fibronectin isolated from porcine plasma can preserve glycans attached on fibronectin.

The inventor has characterized that the structure of sialic acids on porcine fibronectin are Neu5AC and Neu5GC, while that on human fibronectin is only Neu5AC, revealing the possibility of Neu5GC in causing immune response in human body in clinical application. The inventor has confirmed the limited effect of sialic acids of fibronectin in cell adhesion and directed cell migration, so the invention of process for a preparation of a human-used fibronectin isolated from porcine plasma is to release sialic acids from porcine plasma fibronectin.

In addition, the inventor has confirmed that digested plasma fibronectin has a role in positive regulation of cell adhesion and directed cell migration. Therefore, the invention of process for a preparation of a human-used plasma fibronectin with improved wound-healing ability is to digest fibronectin properly into fibronectin peptides after purification procedure.

To solve the problems, this invention provides a method for enhance wound healing in a subject, wherein the method comprising: administering a modified glycosylation fibronectin from porcine by an enzyme to the subject.

In one embodiment of the invention, the modified glycans are a plurality of sialic acid molecules.

In one embodiment of the invention, the plurality of sialic acid molecules are the N-acetylneuraminic acid (Neu5Ac) and/or the N-glycolylneuraminic acid (Neu5GC) residues.

In one embodiment of the invention, the plurality of sialic acid molecules are removed >80%.

In one embodiment of the invention, the enzyme is the α2-3,6,8 Neuraminidase.

In one embodiment of the invention, the enzyme further comprises a proteinase with ability to digest fibronectin.

In one embodiment of the invention, the proteinase is the matrix metalloproteinase 3.

In one embodiment of the invention, the modified glycosylation porcine fibronectin is prepared by an only one gelatin-Sepharose Fast Flow 4B with proper buffer in glycan preservation.

To solve the problems, this invent provides a pharmaceutical composition for enhance wound healing in a subject, wherein the pharmaceutical composition comprising a modified glycans porcine fibronectin by an enzyme, a collagen, a hyaluronic acid a pharmaceutically acceptable salt thereof.

To solve the problems, this invent provides a material for enhance wound healing in a subject, wherein the material comprising a modified glycans porcine fibronectin by an enzyme, wherein the modified glycans are a plurality of sialic acid molecules, wherein the sialic acid molecules are removed >80%, wherein the enzyme is the α2-3,6,8 Neuraminidase.

This invent provides a method for purify the modified glycosylation porcine fibronectin, comprising: step 1, providing a cleared plasma; step 2, passing the cleared plasma through a pre-column of gelatin-Sepharose Fast Flow 4B; step 3, removing nonspecifically adsorbed proteins to the gel with sequential washing with TBS-EDTA; step 4, removing nonspecifically adsorbed proteins to the gel with sequential washing with 1 M NaCl; step 5, removing nonspecifically adsorbed proteins to the gel with sequential washing with <0.5 M Arginine (Arg); step 6, eluting fibronectin sample with >0.5M Arg.

This invent provides a method for modify the glycosylated porcine fibronectin, comprising: step 1, preparing porcine plasma fibronectin (1 mg) in buffer (pH 5-7); step 2, adding 5-50 units α2-3,6,8 Neuraminidase (One unit is defined as the amount of enzyme required to cleave >95% of the terminal α-Neu5Ac from 1 nmol Neu5Acα2-3Galβ1-3GlcNAcβ1-3Galβ1-4Glc-7-amino-4-methyl-coumarin (AMC), in 5 minutes at 37° C. in a total reaction volume of 10 μl); step 3, incubate for 1-24 hours in 37° C.

This invent provide a method for digest glycosylated porcine fibronectin, comprising: incubating modified porcine plasma fibronectin with matrix metalloproteinase-3 (MMP3) overnight at 37° C. at an enzyme-substrate ratio from 1:5 to 1:30.

This invention isolated and modified fibronectin from porcine plasma and demonstrated that modified porcine plasma fibronectin has similar ability as homo plasma fibronectin being as a suitable substrate for stimulation of cell adhesion and directed cell migration.

This invention reveals the applications of modified porcine plasma fibronectin that could be applied as a safe material for clinical wound healing and tissue repair.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the purification method.

FIG. 2 shows the fractions of the washed materials and eluted materials that obtained from the gelatin-Sepharose Fast Flow 4B column.

FIG. 3 shows the percentage of the spectral counts of the glycans with or without sialic acids (Neu5Ac or Neu5GC) relative to the total spectral counts for individual detected N-glycosylation sites.

FIG. 4a-c shows the isolated homo and porcine fibronectin proteins exhibited similar wound closure effect using U2OS, HFF1 and Hela cells.

FIG. 5 shows U2OS cells were plated on coverslips coated with the indicated fibronectin concentration (μg/ml) for 30 min and then the images were taken by phase contrast microscopy. Bar, 100 μm.

FIG. 6 shows the area of cells spreading on coverslips coated with the indicated fibronectin concentration (μg/ml).

FIG. 7 shows U2OS cells were plated on the indicated concentration of fibronectin for 30 min and then their cell attachment was measured. Fold of cells remaining attached on the indicated concentration of fibronectin relative to that on 0 μg/ml fibronectin.

FIG. 8 shows TIRFM images of U2OS cells that had been plated for 1.5 h on coverslips coated with the indicated fibronectin concentration and immunostained with paxillin. Bar, 10 μm.

FIG. 9 shows the sum of the total area of paxillin-marked focal adhesions within a cell versus the fibronectin concentration.

FIG. 10 shows the removal of sialic acids from porcine fibronectin did not affect the cell-fibronectin association.

FIG. 11 shows the MMP3 digestion of porcine fibronectin result.

FIG. 12 shows percentage of wound closure by treating with porcine fibronectin or porcine fibronectin with MMP3.

DETAILED DESCRIPTION OF THE INVENTION

In order to seek safe sources of plasma fibronectin for practical consideration in wound dressing, we isolated fibronectin from human (homo) and porcine plasma and demonstrated that porcine plasma fibronectin has similar ability as homo plasma fibronectin being as a suitable substrate for stimulation of cell adhesion and directed cell migration.

This invention further defined N-glycosylation sites and N-glycans on homo and porcine plasma fibronectin. These N-glycosylation modifications on plasma fibronectin that synergistically support integrin-mediated signals are necessary and sufficient in mediating cellular adhesion and directed cell migration. Our study not only determines the important function of N-glycans on both homo and porcine plasma fibronectin mediated cell adhesion and directed cell migration, but also reveals the potential applications of porcine plasma fibronectin that could be applied as a material for clinical wound healing and tissue repair.

Example 1. Materials and Cells

U2OS (human bone osteosarcoma cell line) and Hela (human cervical adenocarcinoma epithelial cell line) were gifts from Prof. R.-H. Chen's laboratory (Academia Sinica, Taipei, Taiwan) and were maintained in DMEM-high glucose (Invitrogen) supplemented with 10% FBS (Invitrogen) and 1% antibiotic solution (penicillin and streptomycin; Invitrogen) under 5% CO2. HFF1 (human foreskin fibroblasts) cells were purchased from ATCC and were maintained in DMEM-high glucose supplemented with 15% FBS and 1% antibiotic solution (penicillin and streptomycin) under 5% CO2. The homo plasma was obtained from human blood donated by blood donors. All methods related to human blood were carried out in accordance with relevant guidelines and regulations. All experiments protocols related to human blood were approved by the Ethics Committee of the Institutional Review Board (IRB) of National Yang-Ming University. Informed consent was obtained from all subjects. The porcine plasma was obtained from CHAISHAN FOODS CO., LTD.

Example 2. Plasma Fibronectin Preparation Procedure

Plasma Fibronectin Purification

This invent provides a method for purify the glycosylation fibronectin from porcine, comprising: step 1, cleared plasma was passed through a pre-column of gelatin-Sepharose Fast Flow 4B; step 2, removing nonspecifically adsorbed proteins to the gel with sequential washing with TBS-EDTA 50 ml; step 3, removing nonspecifically adsorbed proteins to the gel with sequential washing with 1 M NaCl 50 ml; step 4, removing nonspecifically adsorbed proteins to the gel with sequential washing with <0.5 M Arginine (Arg) 50 ml; step 5, eluting fibronectin sample with >0.5M Arg; step 6, dialyzing fibronectin sample with TBS (pH 5-8) for 24 hours at 4° C.; step 7, concentrating fibronectin sample by Vivaspin 20 centrifugal concentrator (Molecular Weight Cut Off: 100 kDa).

Result

This invention used a plasma fibronectin purification method to isolate high quality fibronectin proteins with glycans preservation from porcine plasma. Plasma was loaded into a pre-column of gelatin-Sepharose Fast Flow 4B. The gel was washed sequentially with TBS-EDTA, 1 M NaCl and <0.5 M Arginine (Arg) to remove non-specific binding proteins, leaving bound fibronectin for elution with >0.5 M Arg. The fractions of eluted fibronectin were pooled and dialyzed in TBS for 48 h at 4° C. and concentrated by Vivaspin 20 centrifugal concentrator (Molecular Weight Cut Off: 100 kDa) (FIG. 1-2).

Plasma Fibronectin Modification

This invent provides a method to modify the glycosylated porcine fibronectin, comprising: step 1, preparing porcine plasma fibronectin (1 mg) in buffer (pH 5˜7); step 2, adding 5˜50 units α2-3,6,8 Neuraminidase (One unit is defined as the amount of enzyme required to cleave >95% of the terminal α-Neu5Ac from 1 nmol Neu5Acα2-3 Galβ1-3 GlcNAcβ1-3 Galβ1-4Glc-7-amino-4-methyl-coumarin (AMC), in 5 minutes at 37° C. in a total reaction volume of 10 μl); step 3, incubate for 1˜24 hours in 37° C.

Glycopeptide Identification for Plasma Fibronectin

Precipitated fibronectin protein pellets (˜10 □g) were subjected to protein digestion using a protocol with trypsin. The digested peptide mixtures were dissolved in 0.1% formic acid and then analyzed using a Dionex Ultimate 3000 nanoLC system (Thermo Scientific) interfaced to an Orbitrap Fusion Tribrid mass spectrometer (Thermo Scientific) equipped with a PicoView nanosprayer (New Objective). The peptides were loaded directly onto a 25 cm×75 □m C18 column (Acclaim PepMap® RSLC, Thermo Scientific) and separated using a 120-min linear gradient of 100% mobile phase A (0.1% formic acid in water) to 40% mobile phase B (acetonitrile with 0.1% formic acid) at a flow rate of 300 nL/min. The eluted peptides were detected in the positive ion mode using a nanospray source. The mass spectrometer was programmed in the data-dependent mode over 3 secs, which consisted of a cycle of one full-scan mass spectrum (400-2000 m/z) on the Orbitrap scan with 120,000 resolution at m/z 400 and an automatic gain control (AGC) target at 200,000 followed by quadrupole isolation with higherenergy collisional dissociation (HCD) MS2 at a normalized collision energy of 30%. HCD MS2 fragment ions detected in the Orbitrap analyzer at 30,000 resolution (AGC target at 100,000) with any previously selected ions dynamically excluded for 60 s. For the database search, the MS datasets for homo and porcine plasma fibronectin were performed using the Byonic™ search energy (Protein Metrics, v.2.7.4) against FN1 human or FN1_Sus scrofa from the Swiss Prot (Swiss Institute of Bioinformatics) database, respectively. Protein modifications were set as carbamidomethyl (C) (fixed), deamidated (N) (variable), oxidation (M) (variable) and N-glycan modifications (182 in homo N-Glycan database; 309 in mammalian N-Glycan database). Up to two missed cleavage was allowed. The mass tolerance was set as ±5 ppm for the MS spectra and ±10 ppm for the MS/MS spectra. For glycopeptide identification, the Byonic score was over 100 and the false discovery rate (FDR) was less than 1%.

Result

This invention used α2-3,6,8 Neuraminidase to remove N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5GC) residues on the porcine fibronectin. The results showed that the porcine fibronectin after modification could be used in wound healing and play the same function as homo fibronectin (FIG. 3).

Example 3. Homo and Porcine Plasma Fibronectin Show Comparable Effects in Terms of Cell Adhesion and Migration

Wound Healing Analysis

U2OS, Hela or HFF1 cells growing on tissue culture plates were trypsinized and re-seeded on 10 μg/ml fibronectin-coated 6-well plates in the culture medium for 16 h and then placed in the temperature-controlled and CO2-controlled chamber of a microscope (Axio Observer.Z1, Zeiss) equipped with a 10×0.25 NA objective lens (Zeiss). Time-lapse images were obtained at 15-min intervals over 12 h using an AxioCamMR3 CCD camera operated by the Zen image analysis software (Zeiss). To calculate the percentage of wound closure, the wound area over a 6-h period or a 12-h period of migration was obtained from the time-lapse movies using the Metamorph image analysis software (Molecular Device), and calculated as the ratio of net wound-healing area to the wound area at 0-h after wounding.

Result

To compare the functionalities of the isolated fibronectin from homo and porcine plasma, we carried out wound-healing migration assays using cells that had been plated on the fibronectin-coated plates. This revealed that the isolated homo and porcine fibronectin proteins exhibited similar wound closure effect using U2OS, HFF1 and Hela cells (FIG. 4a-c ). Therefore, homo and porcine fibronectins would seem to possess comparable capabilities in terms of regulating cell migration.

Adhesion Assay

The cell adhesion assays used 96-well plates that had been pretreated with 1% denatured BSA at 37° C. for 1 h and then coated with the indicated concentration of homo or porcine plasma fibronectin. To perform the experiments, U2OS cells growing on tissue culture plates were trypsinized, re-suspended in serum-free medium and then re-seeded on the pre-treated 96-well plates for 10 min or overnight (˜16 h). After incubation, any non-attached cells were removed completely by washing with PBS twice, and adherent cells were fixed with 5% glutaldehyde in H₂O for 25 min at room temperature, flowed by staining with 0.1% crystal violet in H₂O for 25 min at room temperature. After removing any un-bound crystal violet, the crystal violet-labelled adherent cells were solubilized in 50□ solution A (50% ethanol and 0.1% acetic acid in H₂O), and the amount of crystal violet present measured using a Thermo Scientific Multiskan Spectrum at OD 550 nm. The results are presented graphically using Excel software (Microsoft).

Immunofluorescence Staining and Image Analysis

For paxillin staining, the cells were fixed and immunostained using a method previously described. For TIRFM imaging, the cells were mounted on slides with PBS containing N-propyl gallate. TIRFM images were obtained using 100×1.49NA (Oil-Immersion) Plan objective lens (Nikon) using the iLas multi-modal of the TIRF (Roper)/spinning disk confocal (CSUX1, Yokogawa) microscope system equipped with an Evolve EMCCD camera (Photometrics). To determine the adhesion area, TIRFM images of paxillin-stained cells were thresholded to highlight only the FAs and the areas of these regions were recorded using Metamorph. The total area of recorded FAs was summed to give the adhesion area. The results are presented graphically using Excel software (Microsoft).

Cell Spreading Assay and Image Analysis

Cells growing on tissue culture plates were trypsinized and re-seeded on plates coated with the indicated concentration of homo or porcine plasma fibronectin to allow them to adhere and spread (30 min). Next the cells were fixed with 4% paraformaldehyde in PBS for 20 min at room temperature and then imaged using a microscope 22 (Eclipse TS100; Nikon) coupled with a 20×0.45NA objective lens (Nikon) and a WHITE CCD camera operated by ISCapture software (TUCSEN). To calculate the cell spreading area, the cell area was manually circled on the phase images using Metamorph image analysis software (Molecular Device) and the results are presented graphically using Excel software (Microsoft).

Result

To determine whether homo and porcine fibronectins are comparable when regulating adhesion strength, we initially compared the effect of homo and porcine fibronectin on cell spreading and adhesion. The area of cell spreading was measured after 30 min using U2OS cells that had been seeded onto plates coated with increasing concentrations of homo or porcine fibronectin (FIG. 5). The results revealed that the area of cell spreading increased as the concentration of fibronectin increased for both fibronectins (FIG. 6). Cell adhesive capacity was also quantified and this revealed that increasing concentrations of homo or porcine fibronectin promoted cell adherence to fibronectin (FIG. 7). Next, we immunolabelled and visualized the cellular pattern of the FA marker paxillin (FIG. 8) using cells seeded on increasing concentration of homo or porcine fibronectin for 1.5 h. The results showed an increased area of adhesion (μm²) as the concentration of each fibronectin increased; the quantification was in terms of the area of paxillin-marked adhesion (FIG. 9).

To further determine whether sialic acids (Neu5Ac and Neu5GC) on fibronectin do not responsible for the functioning of fibronectin during adhesion enhancement, we first used α2-3,6,8 Neuraminidase (sialidase) to cleave sialic acids from porcine fibronectin (FIG. 3). We found that the removal of sialic acids from porcine fibronectin did not affect the cell-fibronectin association (FIG. 10). Therefore, the sialic acid-trimming glycosylated fibronectin can be used in for novel wound dressing materials in clinical application to enhance wound healing without the possibility of an aberrant immune response caused by the presence of Neu5Gc.

Example 4. Porcine Plasma Fibronectin Shows Better Effects in Wound Closure after Proteinase Digestion

MMP3 Digestion of Porcine Plasma Fibronectin

To have better exposure the glycan structures on porcine fibronectin for better wound closure function. This invent provide a method for modify the glycosylated porcine fibronectin, comprising: incubating porcine plasma fibronectin with MMP3 overnight at 37° C. at an enzyme-substrate ratio from 1:5 to 1:30.

Wound Healing Analysis

U2OS cells growing on tissue culture plates were trypsinized and re-seeded on 10 μg/ml fibronectin or digested fibronectin-coated 6-well plates in the culture medium for 16 h and then placed in the temperature-controlled and CO2-controlled chamber of a microscope (Axio Observer.Z1, Zeiss) equipped with a 10×0.25 NA objective lens (Zeiss). Time-lapse images were obtained at 15-min intervals over 12 h using an AxioCamMR3 CCD camera operated by the Zen image analysis software (Zeiss). To calculate the percentage of wound closure, the wound area over a 12-h period of migration was obtained from the time-lapse movies using the Metamorph image analysis software (Molecular Device), and calculated as the ratio of net wound-healing area to the wound area at 0-h after wounding.

Result

This invention used MMP3 to generate porcine fibronectin peptides (FIG. 11). To compare the effect of digested fibronectin peptides and non-digested fibronectin, we carried out wound-healing migration assays using cells that had been plated on the digested fibronectin peptides- or non-digested fibronectin-coated plates. This revealed that digested fibronectin peptides significantly promote wound closure effect (FIG. 12). Therefore, the fibronectin peptides possess enhanced ability in terms of regulating cell migration. 

What is claimed is:
 1. A pharmaceutical composition for enhance wound healing in a subject, wherein the pharmaceutical composition comprising a modified glycans porcine fibronectin by an enzyme, a collagen, a hyaluronic acid a pharmaceutically acceptable salt thereof.
 2. The pharmaceutical composition according to claim 1, wherein the modified glycans are a plurality of sialic acid molecules.
 3. The pharmaceutical composition according to claim 2, wherein the plurality of sialic acid molecules are the N-acetylneuraminic acid (Neu5Ac) and/or the N-glycolylneuraminic acid (Neu5GC) residues.
 4. The method according to claim 10, wherein the plurality of sialic acid molecules are removed >80%.
 5. The pharmaceutical composition according to claim 1, wherein the enzyme is the α2-3,6,8 Neuraminidase.
 6. The pharmaceutical composition according to claim 5, wherein the enzyme further comprising a proteinase with ability to digest fibronectin.
 7. The pharmaceutical composition according to claim 6, wherein the proteinase is the matrix metalloproteinase
 3. 8. The pharmaceutical composition according to claim 1, wherein the modified glycans porcine fibronectin is prepared by an only one gelatin-Sepharose Fast Flow 4B with proper buffer condition to preserve glycans.
 9. A material for enhance wound healing in a subject, wherein the material comprising a modified glycans porcine fibronectin by an enzyme, wherein the modified glycans are a plurality of sialic acid molecules, wherein the sialic acid molecules are removed >80%, wherein the enzyme is the α2-3,6,8 Neuraminidase.
 10. The material according to claim 9, wherein the enzyme further comprising a proteinase with ability to digest fibronectin.
 11. The material according to claim 10, wherein the proteinase is the matrix metalloproteinase
 3. 